Its latest investment brings Eli Lilly's total outlay in China to nearly $6 billion so far, the company said.
Eli Lilly is infusing $3 billion into its manufacturing operations in China, pledging to set up local production and supply for oral solid drugs as it works on building out capacity for its experimental GLP-1 pill orforglipron. The investment will play out over the next 10 years and involve work with "several" local partners, according to a March 11 press release (Chinese) on Lilly China's official WeChat account. One such collaboration is with Beijing-based CDMO Pharmaron, which will receive a $200 million investment from Lilly to support its technological capabilities and gradually expand its scale “as needed.” Lilly’s head of manufacturing operations, Edgardo Hernandez, called the Pharmaron partnership a “key step in making this commitment take root in China,” adding that the announcement falls on the 30th anniversary of operations at Lilly's plant in Suzhou, China. “Building on the solid capabilities accumulated over the years at our Suzhou plant and our deep collaboration with Jiangsu province, we will continue to expand the existing incretin injection production capacity at our Suzhou plant while adding oral solid dosage form production capacity in Beijing, promoting the localization of manufacturing and supply of key innovations,” Lilly’s China general manager De Helan explained in the release. The company has invested nearly $6 billion into its Chinese operations to date, including numerous supply chain upgrades over the past two years. In 2024, Lilly committed $200 million to the Suzhou site, adding 120 jobs in an expansion meant to increase the supply of its tirzepatide products. The drugmaker has also planted research roots in the region with the Eli Lilly China Medical Innovation Center and Lilly Gateway Labs, which have been positioned to “further deepen Eli Lilly’s century-old business layout in China," chief scientific officer and president of Lilly Research Laboratories Daniel Skovronsky, M.D., Ph.D., has said previously. Meanwhile, Lilly has been hard at work bolstering the supply of its investigational orforglipron ahead of key approval decisions for the oral GLP-1. Lilly reported "pre-launch inventories" worth $1.5 billion as of Dec. 31, 2025, with most of that supply tied to orforglipron, according to a February filing (PDF). The plan is to launch the drug “in many, many countries around the world, as quickly as possible,” Skovronsky said at the J.P. Morgan Healthcare Conference in January, according to Reuters. Although orforglipron’s FDA review in obesity was set to benefit from the receipt of an FDA Commissioner’s National Priority Voucher (CNPV) in November, the agency ultimately pushed its target decision date out to April 10, Reuters and other news outlets reported earlier this year, lengthening the timeline from what could have been a one- to two-month review under the CNPV program. Lilly has submitted the med to drug regulators in over 40 countries, including China’s National Medical Products Administration (NMPA), where Lilly filed for approval at the end of 2025. While the surge in global drug production prompted by last year’s geopolitical uncertainties and threats of U.S. import tariffs is expected to slow in 2026, financial services firm Atradius estimates that China’s pharmaceutical output will grow 6.6% this year. The country has become a hot spot for licensing deals as of late, while several of Lilly’s Big Pharma peers, such as AstraZeneca and Sanofi, have recently made their own multi-billion-dollar manufacturing investments in the region.